Canonical Allele Identifier: PA2825250109
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447829
ClinVar RCV Id: RCV003176651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000715.2:p.Gly489Arg
CA376071554
NM_000724.3:c.1465G>A
CA376071556
NM_000724.3:c.1465G>C